SPORTARREDO GROUP S.C.

FDA Device Registration & Listing · GRUARO Venezia, IT · Registration 8021093

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
8021093
FEI Number
3001048992
Entity Name
SPORTARREDO GROUP S.C.
City/State/Country
GRUARO Venezia, IT
Establishment Address
VIA DELL INDUSTRIA 7, GRUARO Venezia 30020, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SPORTARREDO GROUP S.C. (Owner Number: 8021093)
Owner / Operator Contact Address
VIA DELL'INDUSTRIA 7, --, GRUARO, IT-VE 30020, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

SportarredoKalfasun MHLF1530 SportarredoKalfasun MHLF610 SportarredoKalfasun MHLF1540SE SportarredoKalfasun MHLF1510 KALFASUN SportarredoKalfasun MHLF830 SportarredoKalfasun MHLF640SE SportarredoKalfasun MHLF630 Sportarredo Vega Lux Sportarredo LP3 Sportarredo LP1 Sportarredo MasterSun 360 New Reflector Sportarredo MasterSun 360 Sportarredo LP2 Sportarredo HPO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LEJ Booth, Sun Tan General, Plastic Surgery Class 2 878.4635 2020-02-27
LEJ Booth, Sun Tan General, Plastic Surgery Class 2 878.4635 2020-02-25

Official Correspondent

CLAUDIO MATTIEL

US Agent Details

Michael Gilley Business: IBL ACQUISITIONS LLC d/b/a TANNING SUPPLIES UNLIMITED Email: Michael@tanningsuppliesunlimited.com Phone: (317) 2171700

Related Public Records

Same Entity

SPORTARREDO GROUP S.C.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K875190 Ultra Tan Intl. AB ULTRA TAN PURPLE PRO 1988-01-14

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8021093. Last updated year: 2026. Please use registration number 8021093 when referencing this establishment in official correspondence.
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